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The generic approval pathway for semaglutide: Bioequivalence studies (12-18 months before ANDA submission): The generic manufacturer must demonstrate that its version produces the same blood concentration curve as the brand-name product

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Duplicate entries were resolved through a two-step deduplication protocol 20 : 1) retaining the most recent FDA receipt date (FDA_DT) for identical CASEID entries

We observed no significant changes in the percentage of insulin cells relative to proliferating cells between groups (Figure 1V)

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